Reaction Details |
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Target | RAC-gamma serine/threonine-protein kinase |
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Ligand | BDBM50316183 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_628225 (CHEMBL1109954) |
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IC50 | 3±n/a nM |
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Citation | Rouse, MB; Seefeld, MA; Leber, JD; McNulty, KC; Sun, L; Miller, WH; Zhang, S; Minthorn, EA; Concha, NO; Choudhry, AE; Schaber, MD; Heerding, DA Aminofurazans as potent inhibitors of AKT kinase. Bioorg Med Chem Lett19:1508-11 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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RAC-gamma serine/threonine-protein kinase |
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Name: | RAC-gamma serine/threonine-protein kinase |
Synonyms: | AKT3 | AKT3_HUMAN | PKB gamma | PKBG | Protein kinase Akt-3 | Protein kinase B (Akt 3) | Protein kinase B, gamma | RAC-PK-gamma | RAC-gamma serine/threonine-protein kinase | STK-2 | Serine/threonine-protein kinase AKT | Serine/threonine-protein kinase AKT3 |
Type: | Enzyme |
Mol. Mass.: | 55769.36 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 479 |
Sequence: | MSDVTIVKEGWVQKRGEYIKNWRPRYFLLKTDGSFIGYKEKPQDVDLPYPLNNFSVAKCQ
LMKTERPKPNTFIIRCLQWTTVIERTFHVDTPEEREEWTEAIQAVADRLQRQEEERMNCS
PTSQIDNIGEEEMDASTTHHKRKTMNDFDYLKLLGKGTFGKVILVREKASGKYYAMKILK
KEVIIAKDEVAHTLTESRVLKNTRHPFLTSLKYSFQTKDRLCFVMEYVNGGELFFHLSRE
RVFSEDRTRFYGAEIVSALDYLHSGKIVYRDLKLENLMLDKDGHIKITDFGLCKEGITDA
ATMKTFCGTPEYLAPEVLEDNDYGRAVDWWGLGVVMYEMMCGRLPFYNQDHEKLFELILM
EDIKFPRTLSSDAKSLLSGLLIKDPNKRLGGGPDDAKEIMRHSFFSGVNWQDVYDKKLVP
PFKPQVTSETDTRYFDEEFTAQTITITPPEKYDEDGMDCMDNERRPHFPQFSYSASGRE
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BDBM50316183 |
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n/a |
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Name | BDBM50316183 |
Synonyms: | 4-(2-(4-amino-1,2,5-oxadiazol-3-yl)-6-((R)-2-amino-3-phenylpropoxy)-1-ethyl-1H-imidazo[4,5-c]pyridin-4-yl)-2-methylbut-3-yn-2-ol | CHEMBL1098938 |
Type | Small organic molecule |
Emp. Form. | C24H27N7O3 |
Mol. Mass. | 461.5163 |
SMILES | CCn1c(nc2c(nc(OC[C@H](N)Cc3ccccc3)cc12)C#CC(C)(C)O)-c1nonc1N |r| |
Structure |
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